VPro5
K号: K183018 · 2019-11-01
广告
决定日期2019-11-01
产品代码OYH
咨询委员会DE
请注意，您没有提供具体的医疗设备监管文本内容，因此我无法进行翻译。请提供需要翻译的具体文本，我将根据您的要求进行翻译。
决定实质等同
器械摘要
VPro5 is the device name listed in this FDA 510(k) record. The listed applicant is Propel Orthodontics, LLC. It received FDA 510(k) clearance on 2019-11-01 under 510(k) number K183018. The device is classified under product code OYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VPro5?
VPro5 is a medical device that received FDA 510(k) clearance on 2019-11-01. The listed applicant is Propel Orthodontics, LLC. The 510(k) number is K183018.
When did VPro5 receive FDA 510(k) clearance?
VPro5 received FDA 510(k) clearance on 2019-11-01, under 510(k) number K183018.
Who is the listed applicant for VPro5?
The FDA 510(k) record lists Propel Orthodontics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VPro5?
The FDA product code for VPro5 is OYH.
列明Propel Orthodontics, LLC为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：OYH）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
广告